Tozasertib

Tozasertib

SCHEMBL614528

Cc1cc(Nc2cc(N3CCN(C)CC3)nc(Sc3ccc(NC(=O)C4CC4)cc3)n2)[nH]n1

nearest known ligand 0.78

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

AURKAAURKBAURKC

The experimentally established mechanism targets of Tozasertib. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
AURKB known ✓ Q96GD4 12/20 0.78
AURKA known ✓ O14965 11/20 0.78
AURKC known ✓ Q9UQB9 2/20 0.78
PLK4 O00444 3/20 0.78
RIPK1 Q13546 3/20 0.78
ABL1 P00519 2/20 0.78
BCR P11274 2/20 0.78
BMPR1B O00238 1/20 0.78
STK25 O00506 1/20 0.78
RIOK3 O14730 1/20 0.78
CHEK1 O14757 1/20 0.78
GAK O14976 1/20 0.78
MUSK O15146 1/20 0.78
EPHB6 O15197 1/20 0.78
PDPK1 O15530 1/20 0.78
MAP3K13 O43283 1/20 0.78
DAPK3 O43293 1/20 0.78
MAP3K7 O43318 1/20 0.78
NUAK1 O60285 1/20 0.78
JAK2 O60674 1/20 0.78

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
SCHEMBL12338916 0.93 AURKB (0.77) AURKBAURKAPLK4RIPK1AURKC
SCHEMBL12338737 0.93 AURKA (0.67) AURKBAURKAPLK4RIPK1AURKC
SCHEMBL12338745 0.92 AURKA (0.67) AURKBAURKAPLK4RIPK1AURKC
SCHEMBL12694190 0.92 AURKA (0.66) AURKBAURKAPLK4RIPK1AURKC
SCHEMBL12102753 0.91 AURKA (0.65) AURKBAURKAPLK4RIPK1AURKC
SCHEMBL12338932 0.91 AURKB (0.65) AURKBAURKAPLK4RIPK1AURKC
SCHEMBL13799832 0.91 AURKB (0.65) AURKBAURKAPLK4RIPK1AURKC
SCHEMBL14386533 0.90 AURKA (0.64) AURKBAURKAPLK4RIPK1AURKC
SCHEMBL12338758 0.90 AURKA (0.77) AURKBAURKAPLK4RIPK1AURKC
SCHEMBL12338763 0.90 AURKB (0.72) AURKBAURKAPLK4RIPK1AURKC

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 253 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2009017838-A2 COMBINATIONS OF JAK-2 INHIBITORS AND OTHER AGENTS EXELIXIS, INC. (US) 2009-02-05 WO claimed
US-20240317733-A1 CYCLOPROPANAMINE COMPOUND AND USE THEREOF TAKEDA PHARMACEUTICALS CO (JP) 2024-09-26 US disclosed
US-11872227-B2 Pharmaceutical combinations comprising a histone deacetylase inhibitor and an aurora kinase inhibitor and methods of use thereof ACETYLON PHARMACEUTICALS, INC. (US) 2024-01-16 US disclosed
US-11872227-B2 Pharmaceutical combinations comprising a histone deacetylase inhibitor and an aurora kinase inhibitor and methods of use thereof ACETYLON PHARMACEUTICALS, INC. (US) 2024-01-16 US disclosed
EP-3533797-B1 HETEROCYCLIC COMPOUND TAKEDA PHARMACEUTICALS CO (JP) 2023-12-20 EP disclosed
US-20220365074-A1 METHODS AND SYSTEMS FOR DETERMINING VIRUSES SUCH AS CORONAVIRUSES USING pH ANALIZA, INC. (US) 2022-11-17 US disclosed
US-11357776-B2 Pharmaceutical combinations comprising a histone deacetylase inhibitor and an aurora kinase inhibitor and methods of use thereof ACETYLON PHARMACEUTICALS, INC. (US) 2022-06-14 US disclosed
US-20210179603-A1 CYCLOPROPANAMINE COMPOUND AND USE THEREOF TAKEDA PHARMACEUTICALS CO (JP) 2021-06-17 US disclosed
US-10968213-B2 Cyclopropanamine compound and use thereof TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2021-04-06 US disclosed
US-10928405-B2 Devices and methods for determining and/or isolating cells such as circulating cancer or fetal cells ANALIZA, INC. (US) 2021-02-23 US disclosed
US-20080249079-A1 N2-{[3-(1-methylethyl)isoxazol-5-yl]methyl}-N4-[5-(1-methylethyl)-1H-pyrazol-3-yl]-6-[(1-methylpiperidin-3-yl)oxy]pyrimidine-2,4-diamine; IGF1R modulators; Abl mutant inhibitors; antiproliferative agents; to modulate cellular activities like differentiation, programmed cell death, migration, chemoinvas EXELIXIS, INC. (US) 2008-10-09 US disclosed
US-20080249079-A1 N2-{[3-(1-methylethyl)isoxazol-5-yl]methyl}-N4-[5-(1-methylethyl)-1H-pyrazol-3-yl]-6-[(1-methylpiperidin-3-yl)oxy]pyrimidine-2,4-diamine; IGF1R modulators; Abl mutant inhibitors; antiproliferative agents; to modulate cellular activities like differentiation, programmed cell death, migration, chemoinvas EXELIXIS, INC. (US) 2008-10-09 US disclosed
WO-2008115890-A2 MAPK/ERK KINASE INHIBITORS TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2008-09-25 WO disclosed
US-20080166359-A1 Methods of using MEK inhibitors EXELIXIS, INC. 2008-07-10 US disclosed
WO-2008076415-A1 METHODS OF USING MEK INHIBITORS EXELIXIS, INC. (US) 2008-06-26 WO disclosed
EP-1904498-A1 FUSED HETEROCYCLIC DERIVATIVES AND USE THEREOF Takeda Pharmaceutical Company Limited (JP) 2008-04-02 EP disclosed
WO-2008016192-A2 FUSED HETEROCYCLIC DERIVATIVE AND USE THEREOF TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2008-02-07 WO disclosed
WO-2007087246-A2 JAK2 TYROSINE KINASE INHIBITION MERCK & CO., INC. (US) 2007-08-02 WO disclosed
WO-2007014250-A2 ABL KINASE INHIBITION VERTEX PHARMACEUTICALS INCORPORATED (US) 2007-02-01 WO disclosed
WO-2007004749-A1 FUSED HETEROCYCLIC DERIVATIVES AND USE THEREOF TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2007-01-11 WO disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (7 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20080249079-A1 N2-{[3-(1-methylethyl)isoxazol-5-yl]methyl}-N4-[5-(1-methylethyl)-1H-pyrazol-3-yl]-6-[(1-methylpiperidin-3-yl)oxy]pyrimidine-2,4-diamine; IGF1R modulators; Abl mutant inhibitors; antiproliferative agents; to modulate cellular activities like differentiation, programmed cell death, migration, chemoinvas IGF1R, INSR, ERBB3 AURKB 1423/4885AURKA 1276/4885AURKC 577/4885
US-20210179603-A1 CYCLOPROPANAMINE COMPOUND AND USE THEREOF KDM1A, KDM1B, KDM2A AURKB 3299/4885AURKA 3174/4885AURKC 4251/4885
US-20240317733-A1 CYCLOPROPANAMINE COMPOUND AND USE THEREOF KDM1A, KDM1B, KDM2A AURKB 3252/4885AURKA 3152/4885AURKC 4256/4885
US-20080166359-A1 Methods of using MEK inhibitors BRAF, NRAS, KRAS AURKB 162/4885AURKA 183/4885AURKC 93/4885
US-10968213-B2 Cyclopropanamine compound and use thereof KDM1A, KDM1B, KDM2A AURKB 3299/4885AURKA 3174/4885AURKC 4251/4885
US-11872227-B2 Pharmaceutical combinations comprising a histone deacetylase inhibitor and an aurora kinase inhibitor and methods of use thereof HDAC1, HDAC3, HDAC8 AURKB 15/4885AURKA 23/4885AURKC 7/4885
US-11357776-B2 Pharmaceutical combinations comprising a histone deacetylase inhibitor and an aurora kinase inhibitor and methods of use thereof HDAC1, HDAC3, HDAC8 AURKB 15/4885AURKA 23/4885AURKC 7/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.